Search Results - "SHIHUANG LIAO"

Exome sequencing identifies ZNF644 mutations in high myopia by Shi, Yi, Li, Yingrui, Zhang, Dingding, Zhang, Hao, Li, Yuanfeng, Lu, Fang, Liu, Xiaoqi, He, Fei, Gong, Bo, Cai, Li, Li, Ruiqiang, Liao, Shihuang, Ma, Shi, Lin, He, Cheng, Jing, Zheng, Hancheng, Shan, Ying, Chen, Bin, Hu, Jianbin, Jin, Xin, Zhao, Peiquan, Chen, Yiye, Zhang, Yong, Lin, Ying, Li, Xi, Fan, Yingchuan, Yang, Huanming, Wang, Jun, Yang, Zhenglin

“…Myopia is the most common ocular disorder worldwide, and high myopia in particular is one of the leading causes of blindness. Genetic factors play a critical…”
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Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population by YI SHI, JIA QU, JIANBIN HU, YUANFENG LI, LI CAI, XIAOQI LIU, FANG LU, SHIHUANG LIAO, BIN CHEN, FEI HE, BO GONG, HE LIN, DINGDING ZHANG, SHI MA, JING CHENG, JIE ZHANG, YIYE CHEN, FUXIN ZHAO, XIAN YANG, YUHONG CHEN, YANG, Charles, LAM, Dennis Shun Chiu, XI LI, PEIQUAN ZHAO, FANJUN SHI, ZHENGZHENG WU, YING LIN, JIYUN YANG, SHIQIANG LI, YUNQING REN, ANQUAN XUE, YINGCHUAN FAN, DEAN LI, CHI PUI PANG, QINGJIONG ZHANG, XUEJUN ZHANG, ZHENGLIN YANG, TAM, Pancy Oi Sin, LIANGDAN SUN, XIANBO ZUO, XIANGTIAN ZHOU, XUESHAN XIAO

“…High myopia, which is extremely prevalent in the Chinese population, is one of the leading causes of blindness in the world. Genetic factors play a critical…”
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HTRA1 variant increases risk to neovascular age-related macular degeneration in Chinese population by Lu, Fang, Hu, Jianbin, Zhao, Peiquan, Lin, Ying, Yang, Yang, Liu, Xiaoqi, Fan, Yingchuan, Chen, Bin, Liao, Shihuang, Du, Qiong, Lei, Chuntao, Cameron, D. Joshua, Zhang, Kang, Yang, Zhenglin

“…Age-related macular degeneration (AMD) is a leading cause of irreversible visual impairment in the world. Advanced AMD can be divided into wet AMD (choroidal…”
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An association study of the COL1A1 gene and high myopia in a Han Chinese population by Zhang, Dingding, Shi, Yi, Gong, Bo, He, Fei, Lu, Fang, Lin, He, Wu, Zhengzheng, Cheng, Jing, Chen, Bin, Liao, Shihuang, Ma, Shi, Hu, Jianbin, Yang, Zhenglin

“…Single nucleotide polymorphisms (SNPs) in the collagen type I (COL1A1) gene have been shown to be significantly associated with high myopia in a Japanese…”
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A novel mutation in BBS7 gene causes Bardet-Biedl syndrome in a Chinese family by Yang, Zhenglin, Yang, Yang, Zhao, Peiquan, Chen, Kechun, Chen, Bin, Lin, Ying, Guo, Fuqiang, Chen, Yigong, Liu, Xiaoqi, Lu, Fang, Shi, Yi, Zhang, Dingding, Liao, Shihuang, Xia, Qingyou

“…To describe the clinical features of and identify a novel mutation in Bardet-Biedl syndrome 7 gene (BBS7) in a Chinese family. Nineteen individuals at risk for…”
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Exome Sequencing Identifies ZNF644 Mutations in High Myopia: e1002084 by Shi, Yi, Li, Yingrui, Zhang, Dingding, Zhang, Hao, Li, Yuanfeng, Lu, Fang, Liu, Xiaoqi, He, Fei, Gong, Bo, Cai, Li, Li, Ruiqiang, Liao, Shihuang, Ma, Shi, Lin, He, Cheng, Jing, Zheng, Hancheng, Shan, Ying, Chen, Bin, Hu, Jianbin, Jin, Xin, Zhao, Peiquan, Chen, Yiye, Zhang, Yong, Lin, Ying, Li, Xi, Fan, Yingchuan, Yang, Huanming, Wang, Jun, Yang, Zhenglin

“…Myopia is the most common ocular disorder worldwide, and high myopia in particular is one of the leading causes of blindness. Genetic factors play a critical…”
Get full text